Showing entry for Groenouw's Dystrophies

General Disease Information
BXGD Id	BXGD001188
Disease Name	Groenouw's Dystrophies
Disease CUI Id	C0018245
MeSH Codes	C16   C11
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations